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Treatment Alternatives in iSGS (NoAAC PR-02 Study)

Treatment Alternatives in Adult Rare Disease; Assessment of Options in Idiopathic Subglottic Stenosis North American Airway Collaborative PR-02 Study (NoAAC PR-02 Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02481817
Acronym
NoAAC PR-02
Enrollment
1239
Registered
2015-06-25
Start date
2015-08-28
Completion date
2020-09-10
Last updated
2021-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Subglottic Stenosis (iSGS)

Brief summary

The study is aimed at answering the questions; (1) How well do the most commonly used treatments in iSGS work? and (2) What quality-of-life trade-offs are associated with each approach? With the results of this trial, the investigators hope to provide information to iSGS patients: (1) Given my personal characteristics, conditions, and preferences, what should I expect will happen to me? and (2) What are my options, and what are the potential benefits and harms of these options?

Detailed description

Idiopathic subglottic stenosis (iSGS) is a rare disease in which the trachea narrows for no known reason. Although uncommon (with an estimated incidence of 1:400,000 persons per year), both the disease and its therapies profoundly affect patients' ability to breathe, communicate and swallow. Breathing difficulties (i.e. dyspnea) is the hallmark symptom and the primary cause of death and disability. However, patients can also experience debilitating voice changes and swallowing problems due to the condition or its treatment. People with this disease often require several surgeries per year. A variety of treatments have been advanced to manage iSGS but are generally categorized into: 1) endoscopic dilation of the tracheal stenosis (accomplished with rigid instruments or inflatable balloons); 2) endoscopic resection of the stenosis (with prolonged medical therapy after surgery); or 3) open neck surgery with resection of the affected tracheal segment with end-to-end anastomosis. Each patient can require repeated surgeries to keep their trachea open, which increases odds of treatment side effects and complications. All approaches have unique and often disabling associated side effects, which can significantly affect a patient's quality of life. Because the disease is rare, it is difficult for patients to find good information so that they can understand the spectrum of treatment options. This is particularly difficult because most patients present with severe breathing trouble and need treatment quickly, limiting their ability to explore options. Additionally, there is a general lack of high-quality, reliable, and accessible data to inform individual patient decision-making. Imperfect information and limited evidence on treatment outcomes complicate patient decision-making as they try to balance survival, symptoms, and quality of life considerations. Beyond the gaps in understanding the relative effectiveness of the different treatments available, no studies have explored functional outcomes in iSGS (i.e. how well patients breathe, speak, and swallow after treatments). These endpoints are important to patients and are arguably a primary determinant in decision-making. Direct engagement with patients is critical to understand these quality of life considerations, since patient and physician perspectives aren't always the same. For example, results show that endoscopic dilation is associated with a higher rate of disease recurrence and thus need for repeated surgery. Meanwhile, open tracheal resection is a major surgery with significant immediate perioperative risks and has been associated with alterations in voice and swallowing. Open tracheal resection appears to reduce the risk of disease recurrence, but the degree of benefit, and the trade-offs associated with this approach are unanswered questions. The proposed study from the North American Airway Collaborative (NoAAC PR- 02) is designed to fill this void. Our prospective study will directly compare the effectiveness of standard of care treatments and assess their associated quality of life tradeoffs in iSGS patients.

Interventions

PROCEDUREEndoscopic dilation of subglottic stenosis

This is accomplished with rigid instruments or inflatable balloons.

PROCEDUREEndoscopic resection of the stenosis

This is accomplished with C02 lasers and paired with prolonged medical therapy after surgery.

PROCEDURETracheal Resection

Resection of the affected tracheal segment with end-to-end anastomosis

Sponsors

Patient-Centered Outcomes Research Institute
CollaboratorOTHER
The Cleveland Clinic
CollaboratorOTHER
University of Utah
CollaboratorOTHER
Johns Hopkins University
CollaboratorOTHER
Vanderbilt University
CollaboratorOTHER
University of Virginia
CollaboratorOTHER
Massachusetts Eye and Ear Infirmary
CollaboratorOTHER
Oregon Health and Science University
CollaboratorOTHER
University of Washington
CollaboratorOTHER
University of California, San Francisco
CollaboratorOTHER
University of California, Los Angeles
CollaboratorOTHER
University of California, San Diego
CollaboratorOTHER
University of Colorado, Denver
CollaboratorOTHER
Baylor College of Medicine
CollaboratorOTHER
Louisiana State University Health Sciences Center in New Orleans
CollaboratorOTHER
Charing Cross Hospital
CollaboratorOTHER
University of Alabama at Birmingham
CollaboratorOTHER
University of Wisconsin, Madison
CollaboratorOTHER
University of Michigan
CollaboratorOTHER
University of Nebraska
CollaboratorOTHER
University of Iowa
CollaboratorOTHER
University of Texas
CollaboratorOTHER
Duke University
CollaboratorOTHER
University of North Carolina
CollaboratorOTHER
Augusta University
CollaboratorOTHER
University of Sydney
CollaboratorOTHER
North American Airway Collaborative
CollaboratorUNKNOWN
University of California, Irvine
CollaboratorOTHER
University of Pittsburgh
CollaboratorOTHER
Loma Linda University
CollaboratorOTHER
Stanford University
CollaboratorOTHER
University of Cincinnati
CollaboratorOTHER
Emory University
CollaboratorOTHER
Ohio State University
CollaboratorOTHER
University of Southern California
CollaboratorOTHER
Temple University
CollaboratorOTHER
Medical College of Wisconsin
CollaboratorOTHER
Landspitali University Hospital
CollaboratorOTHER
Bastian Voice Institute
CollaboratorUNKNOWN
NYU Langone Health
CollaboratorOTHER
Mayo Clinic
CollaboratorOTHER
University of Miami
CollaboratorOTHER
University of Rochester
CollaboratorOTHER
Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Greater than 18 years of age. * The lesion must involve the subglottis.

Exclusion criteria

* Less than 18 years of age * Patients without capacity to consent for themselves * History of significant laryngotracheal traumatic injury. * History of endotracheal intubation or tracheotomy within 2 years of presentation. * Major anterior neck surgery. * History of neck irradiation. * History of caustic or thermal injuries to the laryngotracheal complex. * History of a clinically diagnosed vasculitis or collage vascular disease. * Positive antinuclear cytoplasmic antibody titers.

Design outcomes

Primary

MeasureTime frame
Treatment Effectiveness: Time to recurrent procedure3 years
Treatment Effectiveness: Need for tracheostomy3 years

Secondary

MeasureTime frameDescription
QOL3 yearsPatient quality of life assessment: voice (VHI-10)
Patient Reported Outcome3 yearsNon-traditional PRO focused on social support

Countries

Australia, Iceland, United Kingdom, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026